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<eudamedExport entity="devices">
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    <udiDi>08720214004930</udiDi>
    <basicUdiDi>B-08720214004930</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1422C100</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:56.534Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004923</udiDi>
    <basicUdiDi>B-08720214004923</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1422C090</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:50.523Z</lastUpdated>
  </row>
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    <udiDi>08720214004916</udiDi>
    <basicUdiDi>B-08720214004916</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1422C080</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:49.305Z</lastUpdated>
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  <row>
    <udiDi>08720214004909</udiDi>
    <basicUdiDi>B-08720214004909</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1422C060</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:48.105Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004893</udiDi>
    <basicUdiDi>B-08720214004893</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1422C040</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:46.905Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004886</udiDi>
    <basicUdiDi>B-08720214004886</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1620C120</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:40.901Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004879</udiDi>
    <basicUdiDi>B-08720214004879</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1620C100</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:39.700Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004862</udiDi>
    <basicUdiDi>B-08720214004862</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1620C090</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:38.511Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004855</udiDi>
    <basicUdiDi>B-08720214004855</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1620C080</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:37.304Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004848</udiDi>
    <basicUdiDi>B-08720214004848</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1620C060</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:31.294Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004831</udiDi>
    <basicUdiDi>B-08720214004831</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1620C040</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:30.159Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004824</udiDi>
    <basicUdiDi>B-08720214004824</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1420C120</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:28.903Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004817</udiDi>
    <basicUdiDi>B-08720214004817</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1420C100</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:27.707Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004800</udiDi>
    <basicUdiDi>B-08720214004800</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1420C090</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:21.717Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004794</udiDi>
    <basicUdiDi>B-08720214004794</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1420C080</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:20.501Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004787</udiDi>
    <basicUdiDi>B-08720214004787</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1420C060</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:19.300Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004770</udiDi>
    <basicUdiDi>B-08720214004770</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1420C040</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:18.098Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004763</udiDi>
    <basicUdiDi>B-08720214004763</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1618C120</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:12.091Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004756</udiDi>
    <basicUdiDi>B-08720214004756</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1618C100</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:10.896Z</lastUpdated>
  </row>
  <row>
    <udiDi>08720214004749</udiDi>
    <basicUdiDi>B-08720214004749</basicUdiDi>
    <tradeName>Ankura</tradeName>
    <deviceName>Ankura™ Cuff Stent Graft System</deviceName>
    <manufacturerName>LifeTech Scientific (Europe) B.V.</manufacturerName>
    <manufacturerSrn>NL-MF-000005742</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P070401020101</emdnCode>
    <emdnDescription>PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>LE-cuff1618C090</reference>
    <placedOnMarketCountry>Austria</placedOnMarketCountry>
    <lastUpdated>2026-07-01T01:03:09.725Z</lastUpdated>
  </row>
</eudamedExport>